Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Fabian Wöstmann"'
Autor:
Fabian Wöstmann, Roman-Ulrich Müller, Heike Göbel, Thomas Benzing, Jan U. Becker, Malte P. Bartram
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-4 (2019)
Abstract Background Podocyte infolding glomerulopathy (PIG) is a rare histopathologic finding with global infolding of the podocytes into the glomerular basement membrane (GBM), accompanied by microstructures underneath. Described in 2002 for the fir
Externí odkaz:
https://doaj.org/article/7b63444078364cf092af38ca0172f196
Autor:
Alexander Fuchs, Jennifer Dederichs, Sita Arjune, Polina Todorova, Fabian Wöstmann, Philipp Antczak, Anja Illerhaus, Birgit Gathof, Franziska Grundmann, Roman-Ulrich Müller, Thorsten Annecke
Publikováno v:
Clinical Kidney Journal. 16:384-393
Background Vascular abnormalities and endothelial dysfunction are part of the spectrum of autosomal dominant polycystic kidney disease (ADPKD). The mechanisms behind these manifestations, including potential effects on the endothelial surface layer (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50eb6203df3ef409cb0289b72cbfa88b
https://doi.org/10.1093/ckj/sfac229
https://doi.org/10.1093/ckj/sfac229
Autor:
Simon Oehm, Konstantin Steinke, Johannes Schmidt, Sita Arjune, Polina Todorova, Christoph Heinrich Lindemann, Fabian Wöstmann, Franziska Meyer, Florian Siedek, Thomas Weimbs, Roman-Ulrich Müller, Franziska Grundmann
Publikováno v:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
Background Ketogenic dietary interventions (KDI) have been shown to be effective in animal models of polycystic kidney disease (PKD), but data from clinical trials are lacking. Methods Ten autosomal dominant PKD (ADPKD) patients with rapid disease pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::107a055413f5a283c5bca97a22f6df3d
https://pubmed.ncbi.nlm.nih.gov/36423335
https://pubmed.ncbi.nlm.nih.gov/36423335
Autor:
Roman-Ulrich Müller, Malte P. Bartram, Thomas Benzing, Jan U. Becker, Fabian Wöstmann, Heike Göbel
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-4 (2019)
BMC Nephrology
BMC Nephrology
Background Podocyte infolding glomerulopathy (PIG) is a rare histopathologic finding with global infolding of the podocytes into the glomerular basement membrane (GBM), accompanied by microstructures underneath. Described in 2002 for the first time,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1560edcf9d490761ad59c4b895d97dd
http://link.springer.com/article/10.1186/s12882-019-1478-8
http://link.springer.com/article/10.1186/s12882-019-1478-8